ArticleMicrobial ecology2015
Preening as a Vehicle for Key Bacteria in Hoopoes.
Article in Microbial ecology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 23 citations in OpenAlex.
- Environmental factors associated with nesting habits and age shape the composition and connection between skin and uropygial gland microbiomes of birds.The Journal of animal ecology · 2026Article
- The uropygial gland of the European hoopoe as a symbiotic organ.Animal microbiome · 2026Article
- Nesting hoopoes cultivate in their uropygial gland the microbial symbionts with the highest antimicrobial capacity.Scientific reports · 2024Article
- The reproductive microbiome and maternal transmission of microbiota via eggs in Sceloporus virgatus.FEMS microbiology ecology · 2024Article
- Microbial infection risk predicts antimicrobial potential of avian symbionts.Frontiers in microbiology · 2022Article
- Properties, Genetics and Innate Immune Function of the Cuticle in Egg-Laying Species.Frontiers in immunology · 2022Review
- Unveiled feather microcosm: feather microbiota of passerine birds is closely associated with host species identity and bacteriocin-producing bacteria.The ISME journal · 2019Article
- Article
- Ectoparasite Activity During Incubation Increases Microbial Growth on Avian Eggs.Microbial ecology · 2018Article
- Acquisition of Uropygial Gland Microbiome by Hoopoe Nestlings.Microbial ecology · 2018Article
- Microbiome assembly of avian eggshells and their potential as transgenerational carriers of maternal microbiota.The ISME journal · 2018Article
- Nest Bacterial Environment Affects Microbiome of Hoopoe Eggshells, but Not That of the Uropygial Secretion.PloS one · 2016Article
- The Hoopoe's Uropygial Gland Hosts a Bacterial Community Influenced by the Living Conditions of the Bird.PloS one · 2015Article
Corrections and comments
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oily secretions produced in the uropygial gland of incubating female hoopoes contain antimicrobial-producing bacteria that prevent feathers from degradation and eggs from pathogenic infection. Using the beak, females collect the uropygial gland secretion and smear it directly on the eggshells and brood patch. Thus, some bacterial strains detected in the secretion should also be present on the eggshell, beak, and brood patch. To characterize these bacterial communities, we used Automatic Ribosomal Intergenic Spacer Analysis (ARISA), which distinguishes between taxonomically different bacterial strains (i.e. different operational taxonomic units [OTUs]) by the size of the sequence amplified. We identified a total of 146 different OTUs with sizes between 139 and 999 bp. Of these OTUs, 124 were detected in the uropygial oil, 106 on the beak surface, 97 on the brood patch, and 98 on the eggshell. The highest richness of OTUs appeared in the uropygial oil samples. Moreover, the detection of some OTUs on the beak, brood patch, and eggshells of particular nests depended on these OTUs being present in the uropygial oil of the female. These results agree with the hypothesis that symbiotic bacteria are transmitted from the uropygial gland to beak, brood patch, and eggshell surfaces, opening the possibility that the bacterial community of the secretion plays a central role in determining the communities of special hoopoe eggshell structures (i.e., crypts) that, soon after hatching, are filled with uropygial oil, thereby protecting embryos from pathogens.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.